Antepartal and intrapartal fetal monitoring [[electronic resource] /] / by Michelle L. Murray
| Antepartal and intrapartal fetal monitoring [[electronic resource] /] / by Michelle L. Murray |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | New York, : Springer Pub., c2007 |
| Descrizione fisica | 1 online resource (542 p.) |
| Disciplina |
618.3
618.3/2075 618.32075 |
| Altri autori (Persone) | MurrayMichelle (Michelle L.) |
| Soggetto topico |
Fetal monitoring
Fetal heart rate monitoring |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-281-81329-X
9786611813291 0-8261-0483-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Contributors and Corporate Sponsors; Preface; Acknowledgments; Table of Contents; Chapter 1 Fetal and Maternal Monitoring Equipment; Chapter 2 The Baseline, Accelerations, and Decelerations; Chapter 3 Intrinsic Factors that Affect the Fetal Heart Rate; Chapter 4 Extrinsic Factors that Affect Oxygen Delivery and the FHR; Chapter 5 Acid-Base Balance; Chapter 6 Prediction and Prevention of Intrapartal Fetal Asphyxia; Chapter 7 Hemodynamic and Biochemical Fetal Monitoring; Chapter 8 Variations of the Fetal Heart Rate; Chapter 9 Antepartal Fetal Monitoring; Chapter 10 Biophysical Fetal Assessment
AppendixIndex |
| Record Nr. | UNINA-9910453870603321 |
| New York, : Springer Pub., c2007 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Antepartal and intrapartal fetal monitoring [[electronic resource] /] / by Michelle L. Murray
| Antepartal and intrapartal fetal monitoring [[electronic resource] /] / by Michelle L. Murray |
| Edizione | [3rd ed.] |
| Pubbl/distr/stampa | New York, : Springer Pub., c2007 |
| Descrizione fisica | 1 online resource (542 p.) |
| Disciplina |
618.3
618.3/2075 618.32075 |
| Altri autori (Persone) | MurrayMichelle (Michelle L.) |
| Soggetto topico |
Fetal monitoring
Fetal heart rate monitoring |
| ISBN |
1-281-81329-X
9786611813291 0-8261-0483-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Contributors and Corporate Sponsors; Preface; Acknowledgments; Table of Contents; Chapter 1 Fetal and Maternal Monitoring Equipment; Chapter 2 The Baseline, Accelerations, and Decelerations; Chapter 3 Intrinsic Factors that Affect the Fetal Heart Rate; Chapter 4 Extrinsic Factors that Affect Oxygen Delivery and the FHR; Chapter 5 Acid-Base Balance; Chapter 6 Prediction and Prevention of Intrapartal Fetal Asphyxia; Chapter 7 Hemodynamic and Biochemical Fetal Monitoring; Chapter 8 Variations of the Fetal Heart Rate; Chapter 9 Antepartal Fetal Monitoring; Chapter 10 Biophysical Fetal Assessment
AppendixIndex |
| Record Nr. | UNINA-9910782654003321 |
| New York, : Springer Pub., c2007 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Genetic disorders and the fetus : diagnosis, prevention, and treatment / / edited by Aubrey Milunsky MB BCh, DSc, FRCP, FACMG, DCH, Jeff M. Milunsky MD, FACMG
| Genetic disorders and the fetus : diagnosis, prevention, and treatment / / edited by Aubrey Milunsky MB BCh, DSc, FRCP, FACMG, DCH, Jeff M. Milunsky MD, FACMG |
| Edizione | [Seventh edition.] |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley Blackwell, , 2016 |
| Descrizione fisica | 1 online resource (2122 p.) |
| Disciplina | 618.3/2075 |
| Soggetto topico |
Prenatal diagnosis
Fetus - Diseases - Genetic aspects Fetus - Abnormalities - Genetic aspects |
| ISBN |
1-118-98154-5
1-118-98155-3 1-118-98153-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Dedication; Title page; Copyright; Preface; Acknowledgements; List of Contributors; 1 Genetic Counseling: Preconception, Prenatal, and Perinatal; Incidence, prevalence and burden of genetic disorders and congenital malformations; The goal and purpose of prenatal diagnosis; Prerequisites for genetic counseling; Guiding principles for genetic counseling; Preconception genetic counseling; Genetic disorders that threaten maternal health; Maternal genetic disorders that may threaten fetal health and survival; Genetic disorders that pregnancy may aggravate; A history of infertility
Parental carrier of a genetic disorder A family history of a genetic disorder; Consanguinity; Environmental exposures that threaten fetal health; Identification of preconception options; Genetic counseling as a prelude to prenatal diagnosis; Genetic counseling when the fetus is affected; Perinatal genetic counseling; References; 2 Amniocentesis, Chorionic Villus Sampling, and Fetal Blood Sampling; Introduction; Amniocentesis; Chorionic villus sampling; Fetal blood sampling; References; 3 Amniotic Fluid Constituents, Cell Culture, and Neural Tube Defects; Introduction; Amniotic fluid Amniotic fluid cell culture Prenatal diagnosis of neural tube defects (NTDs); References; Additional References; 4 Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis; The incidence of chromosomal abnormalities detected by conventional cytogenetics; Indications for prenatal cytogenetic diagnosis; Interpretation issues: chromosome mosaicism and pseudomosaicism; Interpretation issues: chromosome rearrangements; Interpretation issues: chromosome polymorphisms, common inversions, and other structural variations Interpretation issues: maternal cell contamination Factors affecting diagnostic success rate and accuracy; Technical standards for prenatal cytogenetics laboratories; Conclusion; Acknowledgments; References; 5 Prenatal Diagnosis of Sex Chromosome Abnormalities; Incidence; Patterns of inheritance; Prenatal diagnosis; Turner syndrome; Klinefelter syndrome; Triple X and poly-X syndromes; 47,XYY males; Structural abnormalities of the X chromosome; Structural abnormalities of the Y chromosome; Disorders of sex development; Ovotesticular disorders of sex development; Conclusion; References 6 Molecular Cytogenetics and Prenatal Diagnosis Microdeletions; Subtle/cryptic rearrangements; Identification of marker chromosomes; Structural rearrangements: duplications; Prenatal diagnosis: interphase analysis; Chorionic villus samples; Interphase studies: fetal cells in maternal blood; Interphase analysis: transcervical and uterine cavity samples; Interphase analysis: preimplantation genetic diagnosis; Conclusion; References; 7 Prenatal Diagnosis and the Spectrum of Involvement from Fragile X Mutations; Introduction; Epidemiology; Clinical involvement in those with the full mutation Clinical phenotype in the premutation |
| Record Nr. | UNINA-9910797662503321 |
| Hoboken, New Jersey : , : Wiley Blackwell, , 2016 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Genetic disorders and the fetus : diagnosis, prevention, and treatment / / edited by Aubrey Milunsky MB BCh, DSc, FRCP, FACMG, DCH, Jeff M. Milunsky MD, FACMG
| Genetic disorders and the fetus : diagnosis, prevention, and treatment / / edited by Aubrey Milunsky MB BCh, DSc, FRCP, FACMG, DCH, Jeff M. Milunsky MD, FACMG |
| Edizione | [Seventh edition.] |
| Pubbl/distr/stampa | Hoboken, New Jersey : , : Wiley Blackwell, , 2016 |
| Descrizione fisica | 1 online resource (2122 p.) |
| Disciplina | 618.3/2075 |
| Soggetto topico |
Prenatal diagnosis
Fetus - Diseases - Genetic aspects Fetus - Abnormalities - Genetic aspects |
| ISBN |
1-118-98154-5
1-118-98155-3 1-118-98153-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Dedication; Title page; Copyright; Preface; Acknowledgements; List of Contributors; 1 Genetic Counseling: Preconception, Prenatal, and Perinatal; Incidence, prevalence and burden of genetic disorders and congenital malformations; The goal and purpose of prenatal diagnosis; Prerequisites for genetic counseling; Guiding principles for genetic counseling; Preconception genetic counseling; Genetic disorders that threaten maternal health; Maternal genetic disorders that may threaten fetal health and survival; Genetic disorders that pregnancy may aggravate; A history of infertility
Parental carrier of a genetic disorder A family history of a genetic disorder; Consanguinity; Environmental exposures that threaten fetal health; Identification of preconception options; Genetic counseling as a prelude to prenatal diagnosis; Genetic counseling when the fetus is affected; Perinatal genetic counseling; References; 2 Amniocentesis, Chorionic Villus Sampling, and Fetal Blood Sampling; Introduction; Amniocentesis; Chorionic villus sampling; Fetal blood sampling; References; 3 Amniotic Fluid Constituents, Cell Culture, and Neural Tube Defects; Introduction; Amniotic fluid Amniotic fluid cell culture Prenatal diagnosis of neural tube defects (NTDs); References; Additional References; 4 Prenatal Diagnosis of Chromosomal Abnormalities through Chorionic Villus Sampling and Amniocentesis; The incidence of chromosomal abnormalities detected by conventional cytogenetics; Indications for prenatal cytogenetic diagnosis; Interpretation issues: chromosome mosaicism and pseudomosaicism; Interpretation issues: chromosome rearrangements; Interpretation issues: chromosome polymorphisms, common inversions, and other structural variations Interpretation issues: maternal cell contamination Factors affecting diagnostic success rate and accuracy; Technical standards for prenatal cytogenetics laboratories; Conclusion; Acknowledgments; References; 5 Prenatal Diagnosis of Sex Chromosome Abnormalities; Incidence; Patterns of inheritance; Prenatal diagnosis; Turner syndrome; Klinefelter syndrome; Triple X and poly-X syndromes; 47,XYY males; Structural abnormalities of the X chromosome; Structural abnormalities of the Y chromosome; Disorders of sex development; Ovotesticular disorders of sex development; Conclusion; References 6 Molecular Cytogenetics and Prenatal Diagnosis Microdeletions; Subtle/cryptic rearrangements; Identification of marker chromosomes; Structural rearrangements: duplications; Prenatal diagnosis: interphase analysis; Chorionic villus samples; Interphase studies: fetal cells in maternal blood; Interphase analysis: transcervical and uterine cavity samples; Interphase analysis: preimplantation genetic diagnosis; Conclusion; References; 7 Prenatal Diagnosis and the Spectrum of Involvement from Fragile X Mutations; Introduction; Epidemiology; Clinical involvement in those with the full mutation Clinical phenotype in the premutation |
| Record Nr. | UNINA-9910821681903321 |
| Hoboken, New Jersey : , : Wiley Blackwell, , 2016 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Looking within [[electronic resource] ] : a sociocultural examination of fetoscopy / / Deborah Blizzard
| Looking within [[electronic resource] ] : a sociocultural examination of fetoscopy / / Deborah Blizzard |
| Autore | Blizzard Deborah |
| Pubbl/distr/stampa | Cambridge, Mass., : MIT Press, c2007 |
| Descrizione fisica | xiv, 253 p |
| Disciplina | 618.3/2075 |
| Collana | Basic bioethics |
| Soggetto topico |
Fetoscopy - Social aspects
Social medicine Prenatal diagnosis |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-09894-2
9786612098949 0-262-26874-4 1-4294-9240-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Fetoscopy as lived experience : a closer look -- Why fetoscopy? Why now?: an ethnography of a medical technology and the emotions that fuel it -- Fetoscopy in cultural context : fetal politics, reproductive choice, religious experiences, and maternal blame -- How to create a fetoscopy collective : define the risks and find participants -- Fetoscopy and the single fetus : diagnostic embryofetoscopy, bladder obstruction, amniotic band syndrome, and the technological fix -- Ligation and twins : making and choosing twins in high-risk pregnancy -- Loss and success : social networks and constructing an outcome -- Final thoughts on fetoscopy. |
| Record Nr. | UNINA-9910451989303321 |
Blizzard Deborah
|
||
| Cambridge, Mass., : MIT Press, c2007 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Looking within : a sociocultural examination of fetoscopy / / Deborah Blizzard
| Looking within : a sociocultural examination of fetoscopy / / Deborah Blizzard |
| Autore | Blizzard Deborah |
| Pubbl/distr/stampa | Cambridge, Mass., : MIT Press, ©2007 |
| Descrizione fisica | xiv, 253 p |
| Disciplina | 618.3/2075 |
| Collana | Basic bioethics |
| Soggetto topico |
Fetoscopy - Social aspects
Social medicine Prenatal diagnosis |
| Soggetto non controllato | PHILOSOPHY/Ethics & Bioethics |
| ISBN |
1-282-09894-2
9786612098949 0-262-26874-4 1-4294-9240-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Fetoscopy as lived experience : a closer look -- Why fetoscopy? Why now?: an ethnography of a medical technology and the emotions that fuel it -- Fetoscopy in cultural context : fetal politics, reproductive choice, religious experiences, and maternal blame -- How to create a fetoscopy collective : define the risks and find participants -- Fetoscopy and the single fetus : diagnostic embryofetoscopy, bladder obstruction, amniotic band syndrome, and the technological fix -- Ligation and twins : making and choosing twins in high-risk pregnancy -- Loss and success : social networks and constructing an outcome -- Final thoughts on fetoscopy. |
| Record Nr. | UNINA-9910778147903321 |
Blizzard Deborah
|
||
| Cambridge, Mass., : MIT Press, ©2007 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Medicina dell'eta prenatale : prevenzione, diagnosi e terapia dei difetti congeniti e delle principali patologie gravidiche / / Antonio Luciano Borrelli ... [et al.]
| Medicina dell'eta prenatale : prevenzione, diagnosi e terapia dei difetti congeniti e delle principali patologie gravidiche / / Antonio Luciano Borrelli ... [et al.] |
| Autore | Borrelli Antonio |
| Edizione | [2a ed.aggiornata e ampliata.] |
| Pubbl/distr/stampa | Milano, : Springer, c2008 |
| Descrizione fisica | 1 online resource (599 p.) |
| Disciplina |
618.3
618.3/2075 |
| Soggetto topico |
Fetus - Diseases - Diagnosis
Fetus - Abnormalities Prenatal diagnosis |
| ISBN |
1-281-23186-X
9786611231866 88-470-0688-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Nota di contenuto | Sonoembriologia e studio ecografico dell’organogenesi embrio-fetale -- Difetti congeniti -- Malattie genetiche nella medicina prenatale -- Diagnostica prenatale dei difetti congeniti: tecniche invasive e non invasive -- Screening prenatale, ecografico e biochimico di cromosomopatie -- Malformazioni del sistema nervoso centrale -- Anomalie scheletriche -- Malformazioni facciali -- Cuore fetale normale e patologico -- Malformazioni gastrointestinali -- Anomalie dell’apparato urogenitale -- Utilizzo degli ormoni placentari e fetali in diagnosi prenatale -- Tumori fetali -- Terapia fetale -- Aborto spontaneo ricorrente: nuovi sviluppi Patogenetici, diagnostici e terapeutici -- Malattie infettive in gravidanza -- Complicanze ipertensive della gravidanza -- Alloimmunizzazione Rh e malattia emolitica feto-neonatale -- Idrope fetale non immunologica -- Diabete mellito e gravidanza -- Sorveglianza della gravidanza -- Monitoraggio delle condizioni fetali -- Ecografia 3D/4D in diagnostica prenatale -- Sofferenza fetale -- Patologia degli annessi fetali -- Parto pretermine -- Restrizone della crescita fetale -- Gravidanza ectopica -- Farmaci e gravidanza -- Tossicodipendenze e gravidanza -- Diagnosi prenatale: morale, deontologia e diritto. |
| Record Nr. | UNINA-9910145748303321 |
Borrelli Antonio
|
||
| Milano, : Springer, c2008 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Obstetric Imaging : Expert Radiology Series
| Obstetric Imaging : Expert Radiology Series |
| Autore | Copel Joshua |
| Edizione | [2nd ed.] |
| Pubbl/distr/stampa | Philadelphia : , : Elsevier, , 2018 |
| Descrizione fisica | 1 online resource (xxvi, 721 pages) : illustrations (some color) |
| Disciplina | 618.3/2075 |
| Altri autori (Persone) |
D'AltonMary E
FeltovichHelen GratacosEduard OdiboAnthony O PlattLawrence TutschekBoris |
| Collana | Expert radiology series |
| Soggetto topico |
Congenital Abnormalities - diagnostic imaging
Fetus - abnormalities Prenatal Diagnosis |
| Soggetto genere / forma | Electronic Books. |
| ISBN | 0-323-49736-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Atlas of selected normal images -- Congenital cystic adenomatoid malformation of the lung -- Bronchopulmonary sequestration -- Hydrothorax -- Scimitar syndrome -- Thymus -- Other thoracic tumors and masses -- Abnormal kidney location -- Abnormal kidney size -- Bilateral renal agenesis -- Unilateral renal agenesis -- Renal pelvis dilatation -- Duplicated collecting system -- Posterior urethral valves -- Multicystic dysplastic kidney -- Autosomal recessive (infantile) polycystic kidney disease -- Fetal adrenal abnormalities -- Ambiguous genitalia -- Cloacal abnormalities -- Gastroschisis -- Omphalocele -- Echogenic bowel -- Fetal hepatic calcification -- Abdominal cysts -- Biliary anomalies -- Intestinal obstruction -- Congenital diaphragmatic hernia -- Hepatic anomalies -- Intraabdominal masses -- Megacystis-microcolon-intestinal hypoperistalsis syndrome -- Sacrococcygeal teratoma and fetus in fetu -- Fetal spleen -- Choroid plexus anomalies : cysts and papillomas -- Corpus callosum and septum pellucidum anomalies -- Septooptic dysplasia -- Cortical development and disorders -- Cerebellar anomalies -- Walker-Warburg syndrome -- Holoprosencephaly -- Intracranial hemorrhage, cysts, tumors, and destructive lesions -- Neural tube defects -- Vascular cerebral anomalies -- Ventriculomegaly -- Pregnancy of unknown location, early pregnancy loss, ectopic pregnancy, and cesarean scar pregnancy -- Nuchal translucency -- Introduction -- Atelosteogenesis disorders -- Campomelic dysplasia -- Chondrodysplasia punctata -- DTDST dysplasia (including AOII and achondrogenesis IB) -- FGFR3 disorders : thanatophoric dysplasia, achondroplasia, and hypochondroplasia -- Hypophosphatasia -- Osteogenesis imperfecta -- Radial ray deficiency -- Russell-silver syndrome -- Short rib thoracic dysplasia with or without polydactyly -- Spondyloepiphyseal dysplasia congenita -- Other type II collagen disorders -- Acrofacial dysostosis -- Caudal regression syndrome -- Spinal abnormalities and Klippel-Feil syndrome -- Abnormal hands : focus on the thumbs -- Craniosynostosis -- Clubfoot (talipes equinovarus) and clenched hands -- Clubfoot (talipes equinovarus) -- Cleft lip and palate -- Orbital defects : hypertelorism and hypotelorism -- Choanal atresia -- Micrognathia and retrognathia -- Facial dysmorphism -- Cystic hygroma -- Neck teratoma -- Fetal thyroid masses and fetal goiter -- Congenital high airways obstruction syndrome (chaos) and bronchial atresia -- Ultrasound of normal fetal heart -- Ventricular septal defect -- Atrioventricular septal defect -- Tricuspid atresia -- Ebstein anomaly and tricuspid dysplasia -- Pulmonary stenosis and atresia -- Aortic stenosis and aortic atresia -- Hypoplastic left heart syndrome and mitral atresia -- Aortic coarctation -- Interruption of the aortic arch -- Aortic arch anomalies -- Tetralogy of Fallot -- Transposition of great arteries -- Double-outlet right ventricle -- Common arterial trunk -- Double-inlet single ventricle -- Atrial isomerism -- Anomalies of pulmonary venous return -- Anomalies of systemic venous return -- Cardiomyopathy -- Cardiac tumors -- Arrhythmias -- Placental abruption -- Placenta accreta -- Amniotic band sequence -- Chorioangioma -- Choriocarcinoma -- Placenta circumvallata -- Cord cyst -- Cord varix --
Gestational trophoblastic disease -- Limb-body wall complex -- Placenta previa -- Vasa previa -- Fetal macrosomia -- Beckwith-wiedemann syndrome -- Intrauterine growth restriction -- Amniocentesis -- Cordocentesis and fetal transfusion -- Chorionic villus sampling -- Radiofrequency ablation -- Selective laser photocoagulation -- Fetal shunts -- Multifetal pregnancy reduction -- Open fetal surgery -- Polyhydramnios -- Oligohydramnios -- Lymphedema and lymphatic malformations -- Nonimmune hydrops fetalis -- Immune hydrops fetalis -- Cervical length and spontaneous preterm birth -- Fetal biophysical profile -- Charge syndrome -- Cornelia de lange syndrome -- Fraser syndrome -- Fryns syndrome -- Goldenhar syndrome -- Klippel-Trénaunay-Weber syndrome -- Holt-oram syndrome -- Meckel-gruber syndrome -- Neu-laxova syndrome -- Noonan syndrome -- Pentalogy of cantrell -- Pierre robin sequence -- Poland sequence -- Prune-belly syndrome -- Roberts syndrome -- Cystic fibrosis -- Pontocerebellar disorders -- Tuberous sclerosis -- Sirenomelia -- Smith-Lemli-Opitz syndrome -- Vater association -- Introduction to aneuploidy -- Triploidy -- Trisomy 13 -- Trisomy 18 -- Trisomy 21 -- Turner syndrome (monosomy X) -- Mosaic trisomies 8, 9, and 16 -- 22q2 deletion syndrome -- Chromosome 4p deletion syndrome (Wolf-Hirschhorn syndrome) -- Chromosome 5p deletion syndrome (cri du chat syndrome) -- Miller-Dieker syndrome (17p3 deletion syndrome) -- Chorionicity of multiple gestations -- Monochorionic monoamniotic twin gestations -- Monochorionic diamniotic twin gestations -- Dichorionic diamniotic twin gestations -- Twin-twin transfusion syndrome -- Twin reversed arterial perfusion sequence -- Diagnostic procedures in multiples -- Cytomegalovirus, rubella, toxoplasmosis, herpes simplex virus, and varicella -- Congenital Zika virus syndrome -- Parvovirus b19 infection during pregnancy -- Congenital syphilis -- Ultrasound physics for the clinician -- Elasticity imaging in obstetrics -- Doppler ultrasound evaluation of the fetus and placenta -- Magnetic resonance imaging in obstetrics -- Three-dimensional ultrasound : techniques and clinical applications. |
| Record Nr. | UNINA-9910583466703321 |
Copel Joshua
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| Philadelphia : , : Elsevier, , 2018 | ||
| Lo trovi qui: Univ. Federico II | ||
| ||